A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041196



Internal ID19130415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5769570..5807809hg38UCSC Ensembl
Innerchr11:5790800..5829039hg19UCSC Ensembl
Innerchr11:5747376..5785615hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3838240
hg1938240
hg1838240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510962
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041196
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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